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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448083Generated: October 29, 2026

3-Methyl-2-thenoyl Chloride → HCID 69187233, compound

https://huagongshe.com/reaction/448083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-2-thenoyl ChlorideHCID 2737605—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 69187233HCID 69187233—

Reaction Steps

In a 20 mL vial 3-butyl-2,4,5-trimethylthiazol-3-ium iodide (48 mg in 0.5 mL DMA, 0.16 mmol, 1 equiv.) was added, followed by TEA (38 mg in 0.5 mL DMA, 0.37 mmol, 2.4 equiv.) and the solution went black. DMAP (2 mg in 0.5 mL DMA, 0.016 mmol, 0.1 equiv) was added next, followed by 3-methylthiophene-2-carbonyl chloride (0.9 mL of 0.2M in DMA, 1.2 equiv). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.95 (t, 3 H) 1.34-1.43 (m, 2 H) 1.60-1.71 (m, 2 H) 2.17 (s, 3 H) 2.20 (s, 3 H) 2.47 (s, 3 H) 3.92-3.98 (m, 2 H) 6.13 (s, 1 H) 6.91-6.96 (m, 1 H) 7.46-7.52 (m, 1 H); MS (ESI) m/z 308 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-617d12226a0045c5aa27e785df878154
Source noteuspto-grants-2013_07